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Summary Literature (0)
DOID:0111018 - cone-rod dystrophy 11


Disease Ontology Definition:A cone-rod dystrophy that has_material_basis_in heterozygous mutation in the RAX2 gene on chromosome 19p13.

Synonyms: CORD11

Xenbase Genes : rax2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012483 - cone-rod dystrophy 11

OMIM:
OMIM:610381 - CONE-ROD DYSTROPHY 11; CORD11

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): cone-rod dystrophy (is_a)